Combining chirality with electrochemical activity is an attracting goal for a wide variety of purposes, such as, in the electrochemical field, the ability to discriminate between antipodes, required in sensors designed for the detection of chiral analytes, and the preparation of chiral electrode surfaces for asymmetric redox reactions. So far chirality in organic semiconductors has mostly been introduced by attaching chiral pendants to the electroactive conjugated backbone through suitable linkers; however, this approach usually leads to poor chirality manifestations. In the last years we have been developing a family of electroactive chiral polyheterocycles, where chirality is not external to the electroactive backbone, but inherent to it, resulting from a tailored torsion produced by the periodical presence of atropisomeric, conjugatively active biheteroaromatic scaffolds. The high interconversion energy barrier results in the enantiomers being easily separable and fully stable upon storage, while their intrinsic 3D character, effective conjugation, and C2 simmetry endows them with high and highly regioregular electrooligomerization ability. Chirality is fully transferred to the resulting films: CD spectroelectrochemistry confirms that the electrode surfaces electrodeposited from enantiomers are perfectly specular and highly chiral. Moreover, the surface chirality can be finely modulated by the amount of injected charge (reducing the torsion angle to achieve better p-conjugation), which suggested us the image of a breathing system. A whole palette of members of this innovative class have already been designed,synthesized, and characterized, both as monomers and as electrodeposited oligomer films, changing the biheteroaromatic core, the conjugated side chains, and also inserting further stereogenic elements. The electrochemical properties of the new compound family will be described and discussed., as monomers (both as racemates and pure enantiomers), as well as chiral conducting surfaces obtained by electrochemical deposition.

Inherently chiral electrochemically active molecules and molecular materials: concept, strategy, potentialities / F. Sannicolò, S. Arnaboldi, V. Bonometti, M. Magni, P.R. Mussini, W. Kutner, K. Noworyta, T. Benincori, S. Rizzo, R. Cirilli, M. Panigati, S. Abbate, G. Longhi, E. Castiglioni. ((Intervento presentato al 46. convegno Heyrovsky Discussion : Molecular Electrochemistry in Organometallic Science tenutosi a Castle Třešť (Czech Republic) nel 2013.

Inherently chiral electrochemically active molecules and molecular materials: concept, strategy, potentialities

F. Sannicolò;S. Arnaboldi;V. Bonometti;M. Magni;P.R. Mussini;M. Panigati;
2013

Abstract

Combining chirality with electrochemical activity is an attracting goal for a wide variety of purposes, such as, in the electrochemical field, the ability to discriminate between antipodes, required in sensors designed for the detection of chiral analytes, and the preparation of chiral electrode surfaces for asymmetric redox reactions. So far chirality in organic semiconductors has mostly been introduced by attaching chiral pendants to the electroactive conjugated backbone through suitable linkers; however, this approach usually leads to poor chirality manifestations. In the last years we have been developing a family of electroactive chiral polyheterocycles, where chirality is not external to the electroactive backbone, but inherent to it, resulting from a tailored torsion produced by the periodical presence of atropisomeric, conjugatively active biheteroaromatic scaffolds. The high interconversion energy barrier results in the enantiomers being easily separable and fully stable upon storage, while their intrinsic 3D character, effective conjugation, and C2 simmetry endows them with high and highly regioregular electrooligomerization ability. Chirality is fully transferred to the resulting films: CD spectroelectrochemistry confirms that the electrode surfaces electrodeposited from enantiomers are perfectly specular and highly chiral. Moreover, the surface chirality can be finely modulated by the amount of injected charge (reducing the torsion angle to achieve better p-conjugation), which suggested us the image of a breathing system. A whole palette of members of this innovative class have already been designed,synthesized, and characterized, both as monomers and as electrodeposited oligomer films, changing the biheteroaromatic core, the conjugated side chains, and also inserting further stereogenic elements. The electrochemical properties of the new compound family will be described and discussed., as monomers (both as racemates and pure enantiomers), as well as chiral conducting surfaces obtained by electrochemical deposition.
English
26-giu-2013
Settore CHIM/01 - Chimica Analitica
Settore CHIM/02 - Chimica Fisica
Settore CHIM/06 - Chimica Organica
Presentazione
Intervento inviato
Sì, ma tipo non specificato
Heyrovsky Discussion : Molecular Electrochemistry in Organometallic Science
Castle Třešť (Czech Republic)
2013
46
J. Heyrovský Institute of Physical Chemistry
International Society of Electrochemistry
Convegno internazionale
F. Sannicolò, S. Arnaboldi, V. Bonometti, M. Magni, P.R. Mussini, W. Kutner, K. Noworyta, T. Benincori, S. Rizzo, R. Cirilli, M. Panigati, S. Abbate, G. Longhi, E. Castiglioni
Inherently chiral electrochemically active molecules and molecular materials: concept, strategy, potentialities / F. Sannicolò, S. Arnaboldi, V. Bonometti, M. Magni, P.R. Mussini, W. Kutner, K. Noworyta, T. Benincori, S. Rizzo, R. Cirilli, M. Panigati, S. Abbate, G. Longhi, E. Castiglioni. ((Intervento presentato al 46. convegno Heyrovsky Discussion : Molecular Electrochemistry in Organometallic Science tenutosi a Castle Třešť (Czech Republic) nel 2013.
Prodotti della ricerca::14 - Intervento a convegno non pubblicato
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/224369
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